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Face-to-Face
Feb 03, 2025 – Feb 05, 2025
Don't miss the latest trends, innovations, and best practices in regulatory submissions, information, and document management (RSIDM)!
| Member Early Bird: | Member In-Person Price | Non-Member In-Person Price | |
|---|---|---|---|
| Virtual Event Price | $1,895.00 | $2,195.00 | $2,545.00 |
Face-to-Face
Jun 15, 2025 – Jun 19, 2025
| Member In-Person Price | Non-Member In-Person Price | |
|---|---|---|
| Virtual Event Price | $1,519.00 | $1,979.00 |
Online
Review the CMC sections of regulatory submissions, the FDA inspection process, and how to avoid or minimize 483s (noncompliance) with this on-demand course.
| Member Price | Non-Member Price | |
|---|---|---|
| Virtual Event Price | $1,800.00 | $2,125.00 |
Online
Complete this On-Demand Training Course to learn about FDA regulations and expectations for the content, submission and review of INDs/NDAs, and the importance of regulatory strategy.
| Member Price | Non-Member Price | |
|---|---|---|
| Virtual Event Price | $3,545.00 | $3,870.00 |
Online
Explore FDA's approach to regulation of combination products, the processes to streamline development of single entity, and aligning requirements between drugs and devices.
| Member Price | Non-Member Price | |
|---|---|---|
| Virtual Event Price | $1,400.00 | $1,725.00 |